LAUSR

The ‘Cardiovascular‐Kidney‐Metabolic Syndrome’ which is characterized by multi‐organ dysfunction ultimately resulting in adverse cardiac outcomes, serves to highlight the importance of organ crosstalk in pathophysiology. The cellular metabolism of fructose, regulated by Ketohexokinase‐C with associated inflammatory sequelae, is mechanistically linked with each component of this clinical entity. Fructose metabolism is confined to the Kidney, Liver, and Small Intestine under normal physiological conditions; however, in the context of ischaemia, HIF‐1α induces cardiac expression of Ketohexokinase‐C with consequent organ hypertrophy and dysfunction. This adverse effect of cardiac HIF‐1α accumulation raises concerns over the potential pleiotropic effects of the ‘HIF stabilizing’ inhibitors of Prolyl Hydroxylase currently entering clinical practice for the treatment of anemia in Chronic Kidney Disease, particularly given the increased cardiovascular mortality observed in this patient group. We suggest that pleiotropic effects of ‘HIF stabilization’ on cardiac physiology warrant investigation and, furthermore, that pharmacological inhibition of Ketohexokinase‐C, and therefore fructose metabolism, represents an opportunity to improve cardiac outcomes in the Cardiovascular‐Kidney‐Metabolic Syndrome.